Proposal for advanced classification of brown forest soils in Japan with reference to the degree of volcanic ash additions

Abstract

The advanced classification of brown forest soils (BFS) is based on the specific properties of these soils, including the acid ammonium oxalate extractable aluminum (Al_ox) and lithic fragment contents, as well as their vertical distributions in the soil profile. In the present study, these properties were used to classify BFS, resulting in four types: (1) H-Al_ox-NGv BFS, (2) H-Al_ox-Gv BFS, (3) M-Al_ox BFS, (4) L-Al_ox BFS. H-Al_ox-NGv BFS is derived from volcanic ash characterized by a high Al_ox content and no lithic fragment, whereas L-Al_ox BFS is derived from weathered bedrock and has a low Al_ox content. H-Al_ox-Gv BFS and M-Al_ox BFS are derived from mixtures of volcanic ash and weathered bedrock. H-Al_ox-Gv BFS is characterized by high Al_ox content and many lithic fragments, whereas M-Al_ox BFS has moderate Al_ox content. H-Al_ox-NGv BFS and black soils (BLS) develop from accumulated volcanic ash, as indicated by declining Al_ox and clay content with decreasing depth in the surface horizons, as a result of successive additions of less-weathered volcanic ash to the soil surface.     

Oxalate-soluble compounds of Al, Fe, and Si in soils of cold humid regions as a function of weathering

Original and published data on the contents of X-ray amorphous oxalate-soluble compounds of Al, Fe, and Si in mesomorphic eluvial soils of cold, moderately cold, and moderately warm continental humid and semihumid regions are generalized. The groups of soils developed from mafic igneous, metamorphic, and pyroclastic rocks are considered. It is shown that the content of oxalate-soluble oxides (OSOx) in the horizons of their maximal accumulation varies from less than 1% to 20–30%; the Al_ox/Fe_ox ratio varies from 1 to 6.5. The leading factor dictating the amount and quality of the OSOx in the soils is the presence or absence of volcanic glass in the parent materials. The boundary between the soils with and without volcanic glass corresponds to the OSOx content of 5% and the Al₂O_3ox/Fe₂O_3ox ratio equal to 2. These criteria are more reliable than the Al_ox/Fe_ox ratio used by foreign soil scientists to specify Andosols (Al_ox/Fe_ox > 2). The contents of oxalate-soluble oxides of Al and Fe do not depend on the total contents of these oxides in the parent material and seem to be related to the presence of these elements in minerals with different resistance to weathering. Under the natural conditions described in this paper, the content of OSOx shows a very weak response to zonal (temperature-controlled) climatic changes and/or to changes in the degree of humidity and the continentality of the climate.     

Extractable Al and Si compounds in pale-podzolic soils of the Central Forest Reserve: Contents and distribution along the profile and by size fractions

The profile distributions of oxalate- and pyrophosphate-soluble Al compounds and oxalate-soluble Si compounds in the main horizons of pale-podzolic soils of the Central Forest Reserve and the fractions <1. 1–5, and >5 μm have been considered. In the clay-eluvial part of soil profile, the content of these compounds is differentiated by the eluvial–illuvial type with a clear accumulation in the EL horizon compared to the AEL horizon. This distribution is largely ensured by their differentiation in the clay and fine silt fractions, while an accumulative distribution of mobile Al compounds is observed in fractions >5 μm. The high correlation between the Al and Si contents in the Tamm extracts from the clay and fine silt fractions with the (Al_ox–Al_py)/Si_ox molar ratios, which are in the range of 1–3 in the EL horizon, confirms that mobile compounds are accumulated in these fractions in the form of amorphous aluminosilicates. In the AEL and EL horizons, an additional amount of Al can pass into the oxalate solution from the fine fractions due to the dissolution of Al hydroxide interlayers of soil chlorites. The eluvial–illuvial distribution of mobile Al and Si compounds typical for Al–Fe–humus podzols within the clay-illuvial part of profiles of the soils under study can be considered as an example of superimposed evolution.     

Towards understanding of carbon stocks and stabilization in volcanic ash soils in natural Andean ecosystems of northern Ecuador

Volcanic ash soils contain very large stocks of soil organic matter (SOM) per unit area. Consequently, they constitute potential sources or sinks for the greenhouse gas carbon dioxide. Whether soils become a net carbon source or sink with climate and/or land‐use change depends on the stability of SOM against decomposition, which is influenced by stabilization mechanisms in the soil. To quantify organic carbon stocks and to clarify the importance of chemical and physical soil characteristics for carbon stabilization in volcanic ash soils, we applied selective extraction techniques, performed X‐ray diffraction analysis of the clay fraction and estimated pore‐size distribution of soils under natural upper montane forest and grassland (páramo) in the Ecuadorian Andes. Our results show that organic carbon stocks under both vegetation types are roughly twice as large as previously reported global averages for volcanic ash soils. SOM stabilization is suggested to be dominantly influenced by the following chemical and physical soil characteristics: (i) direct stabilization of SOM in organo‐metallic (Al‐humus) complexes, explaining at most 40% of carbon accumulation, (ii) indirect protection of SOM (notably aliphatic compounds) through low soil pH and toxic levels of Al, and probably also (iii) physical protection of SOM caused by a very large micro‐porosity. Moreover, in the case of the forest soils, inherent recalcitrance of OM itself was responsible for substantial accumulation in ectorganic horizons. Both vegetation types contributed to soil acidification, thus increasing SOM accumulation.     

General Chemical Properties of Brown Forest Soils Developed from Different Parent Materials in the Submontane Zone of the Kanto and Chubu Districts, Japan

It is essential to analyze chemical properties including the amount of various materials and the soil colloid characteristics in forest soils to forecast wood production and the distribution of and variations in the environmental functions of forest soils, such as conservation of stream water and carbon sequestration. Approximately 70% of the forest soils in Japan consists of Brown Forest Soils (BFS), which are considered to be typical zonal soils under the humid-temperate and warm-temperate regime of Japan. BFS were subclassifled into several groups according to the soil moisture environment along the slope and morphological properties. However, even the same type of soil may display different properties depending on the climatic conditions, parent materials and vegetation types. In the present study, the variations in the carbon content, nitrogen content, cation exchange capacity and some properties depending on the parent materials, were clarified by using 34 sola of BFS, and 3 sola of black soils (BLS) for comparison, which were distributed in the submontane zone of the Kanto and Chubu districts in central Japan under the same climatic conditions. We observed differences in the pH, cation exchange capacity, base saturation and clay content among BFS samples derived from various parent materials. The BFS derived from volcanic ash contained obviously larger amounts of carbon and nitrogen than the BFS derived from other parent materials. However, the BFS derived from volcanic ash differed from the BLS derived from volcanic ash in the vertical distribution pattern of carbon and nitrogen. Thus, even in the submontane zone of the Kanto and Chubu districts, the chemical properties of BFS varied considerably with the parent materials. It was concluded that the classification of BFS by the parent materials was useful for evaluating the ability of the BFS, that cover 70% of the forests in Japan, to store various materials.     

Assessing alternative approaches to predicting soil phosphorus sorption

Twenty‐five pasture soils were sampled from high‐rainfall zones of southeastern Australia to examine relationships between soil properties, and between soil properties and P buffering capacity (PBC) measures. Correlations between PBC values and soil properties were generally poor, with the exception of oxalate‐extractable Al (Al_ox) (r ≥ 0.97). Predictions of PBC were further improved when clay, as well as Al_ox, was included in a linear regression model (r² ≥ 0.98). When Al_ox and oxalate‐extractable Fe were excluded from the modelling exercise, a more complex three‐term linear regression model, including pH_H2O, exchangeable H and cation exchange capacity, adequately fitted both PBC values of the 25 soils examined in this study (r² ≥ 0.76). However, the Al_ox, Al_ox plus clay and the three‐term models gave poor predictions of the PBC values when the models were validated using 28 independent soils. These results emphasize the importance of model validation, because predictive models based on soil properties were not robust when tested across a broader range of soil types. In comparison, direct measures of PBC, such as single‐point P sorption measures, are more practical and robust methods of estimating PBC for Australian soils.     

High gradient magnetic separation of some soil clays from Nigeria, Brazil and Colombia.

High gradient magnetic separation was used to fractionate the clay from some tropical soils. Acid-oxalate-extractable iron (Fe_ox) and aluminium (Al_ox) and total carbon were measured in the whole clay, the magnetic fraction and the tailings. The magnetic separation resulted in a wider range of concentrations of these elements than in the whole clays. In each of the clays Fe_ox was greater in the magnetic fraction than in the tailings; Al_ox was more variable. Carbon was also concentrated in the magnetic fraction suggesting that it is associated more with Fe_ox than Al_ox. The relationships between Fe_ox, Al_ox and carbon depend on soil classification and soil age.     

Estimation of the phosphorus sorption capacity of acidic soils in Ireland

The test for the degree of phosphorus (P) saturation (DPS) of soils is used in northwest Europe to estimate the potential of P loss from soil to water. It expresses the historic sorption of P by soil as a percentage of the soil's P sorption capacity (PSC), which is taken to be α (Al_ox + Fe_ox), where Al_ox and Fe_ox are the amounts of aluminium and iron extracted by a single extraction of oxalate. All quantities are measured as mmol kg soil^?1, and a value of 0.5 is commonly used for the scaling factor α in this equation. Historic or previously sorbed P is taken to be the quantity of P extracted by oxalate (P_ox) so that DPS = P_ox/PSC. The relation between PSC and Al_ox, Fe_ox and P_ox was determined for 37 soil samples from Northern Ireland with relatively large clay and organic matter contents. Sorption of P, measured over 252 days, was strongly correlated with the amounts of Al_ox and Fe_ox extracted, but there was also a negative correlation with P_ox. When PSC was calculated as the sum of the measured sorption after 252 days and P_ox, the multiple regression of PSC on Al_ox and Fe_ox gave the equation PSC = 36.6 + 0.61 Al_ox+ 0.31 Fe_ox with a coefficient of determination (R²) of 0.92. The regression intercept of 36.6 was significantly greater than zero. The 95% confidence limits for the regression coefficients of Al_ox and Fe_ox did not overlap, indicating a significantly larger regression coefficient of P sorption on Al_ox than on Fe_ox. When loss on ignition was employed as an additional variable in the multiple regression of PSC on Al_ox and Fe_ox, it was positively correlated with PSC. Although the regression coefficient for loss on ignition was statistically significant (P < 0.001), the impact of this variable was small as its inclusion in the multiple regression increased R² by only 0.028. Values of P sorption measured over 252 days were on average 2.75 (range 2.0–3.8) times greater than an overnight index of P sorption. Measures of DPS were less well correlated with water‐soluble P than either the Olsen or Morgan tests for P in soil.     

Soils of slopes and bottomland positions of the small stream valley in the central forest reserve: Chemical properties and clay mineralogy

Pale-podzolic soils occupying slope positions in a small stream valley are more acidic and contain less pedogenic chlorites in the clay fraction than those soils occupying uplands. These characteristics are thought to be caused by more intensive leaching of matter from eluvial horizons due to intensive lateral interflow of soil water. Soddy-gleyic soils of the stream bottomland are rich in organic matter and have a slightly acidic reaction in the A1 horizon and an alkaline reaction in the calcareous subsoil. Both factors lead to accumulation of Fe_ox and Al_ox supplied to bottomland positions from uplands and slopes and those formed in situ.     

Relationship of soil properties to p‐fixing capacity of soils in northern Idaho

Abstract

Phosphorus sorption studies were conducted on volcanic ash influenced surface horizons of 29 northern Idaho soils. Results show that the amount of P sorbed was significantly correlated with citrate‐dithionite extractable aluminum (r = .64**), but not with Fe. Other significantly correlated soil properties were: percent base saturation (r = ‐.73**), percent clay (r = .42**), and exchangeable acidity (r = .39*).     

Mercury distribution in tephra soil layers in Hokkaido,Japan, with reference to 34,000-year stratification

Abstract

Tephra from volcanic eruptions contains only small amounts of mercury (Hg) right after the eruption because the high temperature at eruption evaporates Hg in volcanic ash. Thus, accumulation of Hg in tephra soil layers during the dormant periods of the volcano may reflect Hg deposition while the layer was exposed to the atmosphere. To estimate sequential changes in Hg deposition, we measured the Hg content and accumulation in tephra layers from 6 sites in Hokkaido known to have many tephra layers derived from volcanic eruptions over a 34,000-year period. Mercury content and accumulation rate in the soil profiles varied widely depending on the tephra. In each tephra layer, the Hg content and accumulation rates increased principally at the upper soil horizons and decreased at the lower depths. The Hg deposition rates calculated from the amount of Hg accumulated in the tephra layers were similar within the same tephra. These characteristics of Hg distribution indicate that Hg deposition accumulated on the surface of each tephra layer during the period the tephra layer was exposed to the atmosphere. Although physicochemical processes such as leaching out, wind erosion, and volatilization might lead to over- and/or underestimation of the deposition rates, our estimated amounts of Hg were markedly higher in the tephra soils after 1,600?year?BP than before that time. The results of this study suggest that tephra layers in Hokkaido offer important implications for understanding of the historical changes in atmospheric Hg deposition.     

Etude de la nutrition potassique du sorgho II‐ incidence du remplacement du potassium par le sodium sur la teneur en acides organiques des feuilles

Abstract

An Investigation was conducted to determine the content and distribution of total and DTPA‐extractable Zn in the genetic horizons of 72 agriculturally important soils from the six major mineral soil areas in Louisiana.

The concentration of total Zn appeared to vary more with the clay constituents of the soils and the amount of the element in the parent materials than with soil depth. The majority of the soils had the largest amounts of total Zn in the subsurface horizons. The range in total Zn for all soils and horizons was from 7.0 to 150.0 ppm.

The DTPA‐extractable Zn in all of the soils and horizons ranged from 0.08 to 4.22 ppm. In the majority of the soil profiles the highest concentration of extractable Zn was in the surface horizons. There was a decrease in the extractable Zn with increasing soil depth. The alluvial soils along the Ouachita and Mississippi Rivers, and the Mississippi Terrace soil areas contained relatively large amounts of DTPA‐extractable Zn.

In some soils the extractable Zn significantly correlated with total Zn. There was also a close relationship between extractable Zn and organic matter content, especially in the Ap horizons.     

The effect of warming on the vulnerability of subducted organic carbon in arctic soils

Arctic permafrost soils contain large stocks of organic carbon (OC). Extensive cryogenic processes in these soils cause subduction of a significant part of OC-rich topsoil down into mineral soil through the process of cryoturbation. Currently, one-fourth of total permafrost OC is stored in subducted organic horizons. Predicted climate change is believed to reduce the amount of OC in permafrost soils as rising temperatures will increase decomposition of OC by soil microorganisms. To estimate the sensitivity of OC decomposition to soil temperature and oxygen levels we performed a 4-month incubation experiment in which we manipulated temperature (4–20 °C) and oxygen level of topsoil organic, subducted organic and mineral soil horizons. Carbon loss (C_LOSS) was monitored and its potential biotic and abiotic drivers, including concentrations of available nutrients, microbial activity, biomass and stoichiometry, and extracellular oxidative and hydrolytic enzyme pools, were measured. We found that independently of the incubation temperature, C_LOSS from subducted organic and mineral soil horizons was one to two orders of magnitude lower than in the organic topsoil horizon, both under aerobic and anaerobic conditions. This corresponds to the microbial biomass being lower by one to two orders of magnitude. We argue that enzymatic degradation of autochthonous subducted OC does not provide sufficient amounts of carbon and nutrients to sustain greater microbial biomass. The resident microbial biomass relies on allochthonous fluxes of nutrients, enzymes and carbon from the OC-rich topsoil. This results in a “negative priming effect”, which protects autochthonous subducted OC from decomposition at present. The vulnerability of subducted organic carbon in cryoturbated arctic soils under future climate conditions will largely depend on the amount of allochthonous carbon and nutrient fluxes from the topsoil.     

Semiquantitative determination of imogolite and Al-rich allophane (Si / Al ≃ 1 : 2) in some volcanic ash soils in San'in region by a combination of thermogravimetry-differential thermal analysis and trimethylsilylation analysis of soil clays

Abstract

A method to determine the contents of imogolite and Al-rich allophane (Sil Al ? 1 : 2) in volcanic ash soils was presented. The method is based on the (1) assessment of the presence of Al-rich allophane in clays by successsive extraction with dithionite-citrate and oxalate-oxalic acid, (2) trimethylsilylation of soil clay with a mixture of hexamethyldisiloxane, HCl, and isopropyl alcohol, and determination of the content of monomeric Si based on the trimethylsilyl derivative of monomeric orthosilicate anion by gas / liquid chromatography, (3) determination of the total content of imogolite and Al-rich allophane based on the content of monomeric Si from imogolite, (4) determination of the imogolite content by Thermogravimetry (TG )-Differential Thermal Analysis (DTA) based on the weight loss due to endothermic dehydroxylation with maximum values at ca. 386°C, (5) calculation of the Al-rich allophane content by subtracting the imogolite content from the total content of these minerals, and (6) evaluation of the imogolite and Al-rich allophane content of soil by multiplying clay content of soil and the two mineral content of clay. The trimethylsilylation analysis was found to be reproducible, and the estimated total amounts of two minerals in clays by this method were adequately approximated to those evaluated from the amount of Si (= Si_o) extracted with oxalate-oxalic acid after extraction with dithionite-citrate. The variation in the abmldance of two minerals in the soil horizons of volcanic ash soils from the San'in region indicated that this method is suitable for the profile-study of volcanic ash soils.     

Evaluation of the BCR sequential extraction for trace elements in European reference volcanic soils

Trace metal behaviour in volcanic ash soils displays distinctive features related to the soils’ large contents of metal‐binding phases and to the rapid release of trace metals from glasses and weatherable minerals. In this work, the BCR (Community Bureau of Reference) sequential extraction scheme (exchangeable + weak acid soluble, reducible, oxidizable, and non‐extractable metal fractions) was applied to selected COST‐622 European reference volcanic soils to determine partitioning of zinc and copper between various solid‐phase constituents, along with the major elements Al, Fe and Mn. The total extracted Al (ΣAl) was strongly correlated with acid ammonium oxalate extractable Al (Al_o) (ΣAl = 0.985Al_o+ 0.11, R²= 0.98), while the total extracted Fe clearly underestimated the amorphous fraction. Large values for the non‐extractable Al fraction were associated with the presence of gibbsite and phyllosilicates. Although the Zn and Cu contents of the soils were generally large, total amounts extracted (the potentially mobilizable fraction) were small, especially for Zn and for soils with crystalline secondary minerals. The fraction of the total Cu which was potentially mobilizable generally exceeded that of Zn. In the potentially mobilizable Cu the oxidizable fraction was generally dominant. Biocycling appears to play an important role in the surface enrichment of potentially mobilizable Zn and Mn. Although further methodological research seems necessary, the BCR sequential extraction appears to be a valuable tool for studies on metal dynamics in soils with andic properties.     

The mineralization rate of black soil carbon in the deep layers of Japanese volcanic ash soil may be easily accelerated by labile carbon supply

ABSTRACT

The stability of black soil carbon in the deep layers of Japanese volcanic ash soil (i.e., buried A horizons) is often explained by its unique chemical (molecular structure) and physical (associated with short-range-order minerals) recalcitrance. However, the stability of black soil C in buried A horizons may be changed by labile C supply for soil microbes. Here, we hypothesized that the mineralization of black soil C in buried A horizons of Japanese volcanic ash soil could be easily accelerated by a supply of labile C (i.e., a priming effect; PE). To test our hypothesis, we investigated the direction and magnitude of the PE with a buried A horizon in Japan using ¹³C-labeled glucose (2.188 atom %) in a short-term (21 days) incubation study. We also investigated the effect of mineral nitrogen (N), which could contribute to microbial activity in this incubation study. We found that a positive PE occurred by glucose supply with (182%) or without (181%) mineral N input over the 21-day incubation, and its values were very similar to the PE ratios previously reported in other deep soils. The estimated mean residence time (MRT) of black soil C considering PE was clearly accelerated by glucose supply, regardless of mineral N input, compared with the initial soil MRT. These results strongly support our hypothesis that the mineralization rate of black soil C in buried A horizons is easily accelerated by a labile C supply, and it also demonstrates important implications for the effects of global warming on buried A horizons (e.g., increased root exudation, fine root biomass supply, and N deposition) in Japanese volcanic ash soils.     

Phosphorus sorption by Andepts from the Southern Highlands of Papua New Guinea

P sorption curves (18 hours, 0.01 M CaCl₂) were determined for various A, AB, B and C horizons of six Andepts. Two of these soils were formed in alluvially sorted and redeposited volcanic ash. P buffer capacity (PBC) and equilibrium solution P concentration (EPC) were derived from the curves. PBC was high for all samples indicating large sorption capacities. Soils formed in alluvial ash had lower PBC than those developed in airfall ash. In the latter soils, PBC was affected by degree of weathering. Multiple regression indicated that most variation in PBC was accounted for by citrate-dithionite minus pyrophosphate extractable Al, oxalate minus pyrophosphate extractable Al, and pyrophosphate extractable Fe. This suggests that allophane, crystalline and non-crystalline aluminium hydrous oxides, and Fe associated with organic matter, account for the predominant P-sorbing sites. The low EPC figures, which were correlated with Olsen extractable P, indicate potential P deficiency as a limitation to crop production.     

Mercury distribution in tephra soil layers in Hokkaido, Japan, with reference to 34,000-year stratification

Tephra from volcanic eruptions contains only small amounts of mercury (Hg) right after the eruption because the high temperature at eruption evaporates Hg in volcanic ash. Thus, accumulation of Hg in tephra soil layers during the dormant periods of the volcano may reflect Hg deposition while the layer was exposed to the atmosphere. To estimate sequential changes in Hg deposition, we measured the Hg content and accumulation in tephra layers from 6 sites in Hokkaido known to have many tephra layers derived from volcanic eruptions over a 34,000-year period. Mercury content and accumulation rate in the soil profiles varied widely depending on the tephra. In each tephra layer, the Hg content and accumulation rates increased principally at the upper soil horizons and decreased at the lower depths. The Hg deposition rates calculated from the amount of Hg accumulated in the tephra layers were similar within the same tephra. These characteristics of Hg distribution indicate that Hg deposition accumulated on the surface of each tephra layer during the period the tephra layer was exposed to the atmosphere. Although physicochemical processes such as leaching out, wind erosion, and volatilization might lead to over- and/or underestimation of the deposition rates, our estimated amounts of Hg were markedly higher in the tephra soils after 1,600 year BP than before that time. The results of this study suggest that tephra layers in Hokkaido offer important implications for understanding of the historical changes in atmospheric Hg deposition.     

Mineralogical properties of andisols of the Kitakami mountain range,Northeastern Japan

We studied the mineralogical properties of Andisols of the Kitakami mountain range. Soils of the northern and central parts of the mountain range contained higher levels of acid oxalate extractable silicon (Si_o), aluminum (A1_o), and iron (Fe_o) but smaller amounts of sodium pyrophosphate-extractable aluminum (Al_p), iron (Fe_p), and carbon (C_p) than those of the southern part. Consequently, the soils of the northern and central parts of the mountain range contained large amounts of allophane and ferrihydrite whereas in the soils of the southern part A1 (Fe)-humus complexes and 2:1 and 2:1:1 clays predominated. The amount of sand (20-2,000 μm) in the soils tended to decrease sharply from the north to the south of the mountain range. The soils of the northern and central parts of the mountain range contained larger amounts of heavy minerals in their fine sand fraction (20-200 μm). The soils of the southern part, on the other hand, contained larger amounts of fine-grained quartz (2-20 μm). All the soils of the mountain range contained substantial amounts of volcanic glass in their sand fraction. However, on a total soil basis, the amount of volcanic glass in the soils decreased from the north to the south of the mountain range and the trend was parallel to that of the sand content of the soils. From these results, we concluded that (i) the soils of the northern and central parts of the mountain range were derived mainly from tephras and (ii) the soils of the southern part were strongly influenced by long-range eolian dust.     

Sesquioxidic components of selected Taiwan soils

Twenty two surface soils, representing six parent materials and four soil groups, were sampled in Taiwan for the present study.Except in the soil derived from volcanic ash, the sesquioxidic components and relatively easily extractable Si were present only in small amounts in the NaOAc and H₂O₂- NaOAc extractable fractions. In addition to Fe, both Si and Al were present in the dithionite-citrate-bicarbonate extracts in considerable amounts, indicating that Si and Al were either present separately or in association with Fe in the sesquioxidic fractions of the soils. The amounts of Si, Al and Fe extracted by the dithionite-citrate-bicarbonate and boiling KOH treatments differed from sample to sample, indicating that they are important variables in the nature of the soils studied.The amounts of the ammonium oxalate-extractable Al and Fe, representing the noncrystalline sesquioxidic products of relatively recent weathering, also differed with parent materials and pedogenic processes. The statistical data indicate that the ammonium oxalate-extractable Al and Fe are related to the contents of organic matter but not to acidity and the contents of clay. The percentage distribution of the extractable Al in the > 2 μm fractions of the selected soil samples ranged from 22.0 to 52.5% and that of the extractable Fe from 11.1 to 38.1%, indicating that the active non-crystalline Al and Fe components in the non-clay fractions deserve close attention in the study of pedogenesis and other soil physicochemical reactions in relation to soil fertility and environmental protection.